Defects and Disorders in Hafnium Oxide and at Hafnium Oxide/Silicon Interface Hei Wong City University of Hong Kong Email: heiwong@ieee.org Tokyo MQ2012 1
Outline 1. Introduction, disorders and defects 2. Intrinsic oxygen vacancies 3. Oxygen Interstitials 4. Grain boundary states 5. Extrinsic i defects (water-related defects) 6. Interface traps 7. Conclusions Tokyo MQ2012 2
1. Disorders and defects are often localized states which can trap electrons or holes and are often termed as trapping centers or simply traps ; give rise to various reliability issues, such as V T shift, gate leakage, NBTI, PBTI and dielectric breakdown. They are quite clear in silicon oxide, but still not be fully explored in most high-k materials! Tokyo MQ2012 3
1. Defects and disorders Bonding: Hf atom has 4 valence electrons given by 5d 2 6s 2, each Hf atom in the HfO 2 is coordinated to four O atoms. An O atom has 6 valence electrons (s 2 p 4 ), thus each O atom bridges with two Hf atoms in HfO 2. Crystal structure: amorphous/unique form of crystal modification. Impurities: In the form of as network sites or interstitials. Perfect material: all atoms in the material did not deviate from their regular coordination numbers. Tokyo MQ2012 4
1. Disorders and defects In stoichiometric oxides, the atomic disorders always exist. Disorders can be due to cation or anion vacancies (Schottky disorders), or interstitial atoms (Frenkel disorders). Oxygen Vacancies (V O ): most metal oxides are often found to be (slightly) non-stoichiometric and are oxygen deficient. Formation energy of V O and oxygen interstitial are smaller than that for the defects at the metal sites. V O is primary source of intrinsic defects. Grain boundary states: localized states near the E C associated with the grain boundaries TM/RE oxides with anocrystallites. Impurities: the impurities from the deposition precursors result in the formation of structural imperfections i or interstitial i i trapping centers. Tokyo MQ2012 5
2. Intrinsic oxygen vacancies Why? Large chance for incomplete oxidation and leads to a higher amount V O because of the low oxidation temperatures t for metals (< 700 o C). High-k oxides are more ionic and less stable. Annealing of the TM/RE oxide in inert gases or in vacuum would result in the decomposition of M-O bonds and would give rise to more V O. How? High-k V O centers have a strong localization effect because of the ionic bonding and the strong localization of the defect wavefunctions on the neighboring metal ions. The localized states may be either near the band edges or can be deep states. HfO 2 V O is in the upper mid-gap of Si. It can trap electrons and induce instability of MOS device operation. Tokyo MQ2012 6
2. Intrinsic oxygen vacancies Formation The formation energy required to form an V O in an O 2 ambient in a TM/RE oxide is generally much smaller than the covalent dielectrics because of the higher energy level of O vacancies in the ionic oxide. V O formation may also result in the generation of excess electrons in the conduction band. V O in HfO 2 film may be formed through the following two reactions: HfO 2 V O 2+ + ½ O 2 G 1 (a) HfO 2 V 2+ O +2e + ½ O 2 G 2 (b) For the energy point of view, reaction (b) is more favorable. Tokyo MQ2012 7
2. Intrinsic oxygen vacancies Evidence of V O in PL Spectra E V to V O transition Short-wave absorption edge in the excitation PL spectrum of HfO 2 film can be attributed t to transition from valence band to the O vacancy levels. The vacancy zone is formed below of E C. PL of as-deposited (dotted) and annealed (line) HfO 2. The position of the absorption edge agrees with the position of the O vacancy levels with respect to The HfO 2-x valence band. Tokyo MQ2012 8
V O Reduction with N Incorporation of N atoms into a metal oxide film can suppress the vacancies effectively. Pronounced reduction in the flatband shift of the temperaturedependent C-V characteristics was found. Leakage current can be reduced remarkably due to the suppression of the V O centers. Tokyo MQ2012 9
2. Intrinsic oxygen vacancies N fills up the V O center, replaces the nearest neighbor O site to V O and make the V O centers inactive. The two electrons trapped at the V O level are transferred to N 2p orbital at the top of the valence band and the V O related gap state disappears. The neutral V O0 is converted into positively charged V 2+ O2. Tokyo MQ2012 10
3. Oxygen interstitials According to the theoretical calculation by Foster et al., both atomic and molecular incorporation of O into monoclinic HfO 2 are possible but atomic O incorporation is more energetically favorable. For atomic O incorporation, the O I can be in the form of either a fourfold-coordinated tetragonally or threefoldcoordinated trigonally. The interstitial O atoms and molecules can trap electrons from injected from Si. The charged defect species are more stable than neutral species. Tokyo MQ2012 11
4. Grain boundary states Evidence of GB States For as-deposited samples, most of the trapped charges cannot be discharged in the detrapping experiment indicating the presence of a large amount of O vacancies in the film. At 700 o C, almost all trapped charges were de-charged indicating that most of deep V O states have been suppressed. But 700 o C annealed sample was found to have a lot of shallow states which are attributed to the present of large amount of grain boundary shallow traps. Tokyo MQ2012 12
5. Extrinsic defects: Water-related related defects The Sources TM/RE oxides are easier to be contaminated by foreign atoms. The precursors used for the CVD or ALD processes generally contain: carbon, hydrogen and oxygen, thus, water and other byproducts often contaminate the films. Water-related groups are found in HfO 2 films. Even with prolonged high-temperature annealing, it was found that the H 2 O and OH groups are still detectable. Forming gas annealing for reducing the defect density is actually involved the passivation of dangling defects with H. Tokyo MQ2012 13
5. Extrinsic defects: Water-related related defects The Effects: In high-k TM/RE oxide, the passivation of V O results in the formation of more stable V O -H complex which is a positive fixed charge in the film. This is one of the reasons for high positive fixed charge in The HfO 2. Hydrogen atoms may also be incorporated into the dielectric i films as interstitials titi and bonded d to threefoldcoordinated O atoms. When hydrogen is bonded to a fourfold-coordinated O of the oxide network, one of the four metal-o bonds is nearly broken. H atoms can be released under high-field or hot carrier stressing and has been proposed as a mechanism for defect generation. Tokyo MQ2012 14
5. Extrinsic defects: Water-related related defects Evidence of IR : Organic fragments + OH OH H 2 O Infrared spectrum of the HfO 2 film prepared by ALD method. Tokyo MQ2012 15
5. Extrinsic defects: Water-related related defects Evidence of PLE: The PL intensity of this peak increases remarkably by using 5.1 ev photon excitation which is able to break the H-OH bonds in the water molecules. The decomposition of water molecule in The HfO 2 films upon photon absorption can be described by: H * 2 O + h OH + H where OH * is radical in the electronic-excited it state. t Tokyo MQ2012 16
5. Extrinsic defects: Water-related related defects Mechanisms In the TM/RE oxides, water can be incorporated into the films during the film deposition via the oxygen vacancies according to: H 2 O (gas) + V O + + + O O 2(OH) O + The double negatively-charged oxygen anion is converted in to a positively-charged ii (OH) + O where the oxygen has a single negative charge. Since the OH - anions in the oxygen lattice points are loosely-coupled with H atoms, they can hop over the film via the defects. As the absorption energy of H 2 O molecules is closed to the band-toband transition energy, the energy is able to set the water into excited state (H 2 O*) and result in the radiation and dissociation of the water molecules l into О*, H*, OH, or OH + fragments. Tokyo MQ2012 17
12 10 10.19 C 2 D 2-8 8.66 B 2 H 2 O H + OH* (A 2 ) Energy (e ev) 6 4 4.06 A 2 (excited OH* state) 4.0 ev PL 2 H + OH* (A 2 ) H 2 O + OH(Х 2 i ) + h 0 X 2 i A vibronic transition model was proposed for the OH defect state conversion. Tokyo MQ2012 18
6. Interface traps At high-k/si interface: -- the interface stress is much larger; -- the bond strengths are much weaker; -- larger thermal expansion coefficients of the high-k materials. high interface trap density! Formation of a silicate layer at the interface will help to release the interface strain and thus improve the interface properties. Proper thermal annealing may allow the film to relax to a less-strained strained interface by forming metal-si bonds, Si-O bonds, and random bonding silicates in the transition layer. The role of O! Tokyo MQ2012 19
6. Interface traps: Role of Oxygen Oxygen is always good except EOT! Oxygen permeability of the thin metal oxide film is quite high and lead to interface oxidation. The interface oxidation reactions leads to the formation of SiO 2 or silicates, but it is still difficult to convert the silicide bonds to oxide or silicate bonds. The vacancy levels in silicates should be slightly different to the elemental oxides as the vacancy site may have both metal and Si neighbors. Tokyo MQ2012 20
6. Interface traps: Role of Si Si can be easily incorporated into the metal oxide networks, particularly at the oxide/si substrate interface. made the interface bonding configuration even more complicated. Tokyo MQ2012 21
N Doping on HfO 2 : interface improvement Hf-N is in a 4-fold coordination reduce the average atomic coordination number. Tokyo MQ2012 22
HfO 2 Nitrogen Doping Steeper slope low interface trap density Tokyo MQ2012 23
7. Conclusions Causes The defect and disorder states of hafnium oxide (and other high-k materials) and their impacts are much more complicated than the conventional SiO 2. The (Hf, Si, O) ternary interface leading to: Si-O O, Hf-O O, and Hf-Si bondings. Si diffusivity in HfO 2 is high. Bulk silicate is not uncommon. The deposition process causes the introduction ti of significant amount of extrinsic defects and high amount of V O. The deposition/annealing conditions make substrate Si to out diffusion, make bulk O to diffuse into the substrate. Tokyo MQ2012 24
7. Conclusions Bulk Oxygen vacancy is the major source of bulk trap. Shallow traps arise from the grain boundary states of the nanocrystllite phases. Interface Metallic bonding has to be avoided. Silicate bonding is more favorable. Stress could be the deterministic factor. At high-k/si interface, the interface stress is much larger and the bond strengths are much weaker; these lead to the high interface trap density. Formation of a silicate layer at the interface will help to release the interface strain and thus improve the interface properties. Tokyo MQ2012 25
7. Conclusions Measures Proper thermal annealing may allow the film to relax to a less-strained interface by forming metal-si bonds, Si-O bonds, and random bonding silicates in the transition layer. Some process, such as N and Al doping looks promising for overcoming the effects of defect states in high-k based transistors. Metal gate thickness control and CeO 2 capping which control the oxygen supply to the gate dielectric film (see M. Kouda, Ph.D. Thesis) will also help to control the oxygen vacancies and interface structure. Tokyo MQ2012 26
How about La 2 O 3? Tokyo MQ2012 27
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